A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965771



Internal ID22740706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56864497..56864497hg38UCSC Ensembl
chr6:56729295..56729295hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441094
Samples
Known GenesDST
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965771
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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